ライフサイエンスコーパス: hatchling

1 spring (lay larger eggs, which yield heavier hatchlings).

2 torecipient structures resembled that of the hatchling.

3 before and after colonization of 1,500 squid hatchlings.

4 as has been hypothesized for precocial bird hatchlings.

5 ment and produce many small eggs and smaller hatchlings.

6 n of auditory preferences in precocial avian hatchlings.

7 eding field plots with rare and common giant hatchlings.

8 alis and E. faecium kill C. elegans eggs and hatchlings, although only E. faecalis kills the adults.

9 is the change from fully toothed jaws in the hatchling and juvenile individuals to a completely tooth

10 present in the white and yellow bands of the hatchling and they gradually perish in the adult skin.

11 les with fresh semen (n = 10) resulted in 80 hatchlings and 27.6% fertility.

12 examined after unilateral cochlea removal in hatchlings and 3-week-old birds.

13 n both T. scripta and C. caretta 1-2 day-old hatchlings and 90% reliable for identifying sex in 83-17

14 was restricted to the liver and intestine of hatchlings and adult zebrafish, whereas zRetSat B was ex

15 tions of olfactory sensory neurons (OSNs) in hatchlings and adults responded with similar tunings to

16 uronal cell population in the optic lobes of hatchlings and adults, we reveal a switch towards dopami

17 tions give rise to the banded pattern of the hatchlings and black spot formation is an intrinsic capa

18 characterized by uniform black coloration in hatchlings and black spots in adulthood; we establish th

19 ing success of each clutch, and assessed all hatchlings and dead embryos for gross morphological malf

20 n = 4) and 48 h (n = 1) semen resulted in 17 hatchlings and fertilization rates of 28.1% and 7.1% res

21 caretta), which leave their home beaches as hatchlings and migrate across entire ocean basins before

22 presence of three components in UV cones of hatchlings and terrestrial adults ruled out a developmen

23 to assess global trends in the sex ratio of hatchlings and the extent to which feminisation is drivi

24 pment of the banded pattern of leopard gecko hatchlings and the transition to black spots in the adul

25 expression and polysiaylation in embryonic, hatchling, and adult chick corneas.

26 icity is limited in native populations where hatchlings are not targeted by cannibalistic tadpoles.

27 The blue tail colors of hatchlings are produced by incoherent scattering from pr

28 Caenorhabditis elegans hatchlings arrest in a dormant state termed "L1 diapause

29 ells become necrotic and kill E. solidaginis hatchlings before gall induction.

30 hydrodynamic simulations, we show that these hatchling behaviors nearly tripled diffusivity and made

31 Newborns and hatchlings can perform incredibly sophisticated behavior

32 (NO) has been implicated in learning in the hatchling chicken.

33 studied in the vestibular nuclei of 4-5-day hatchling chicks by using single and double labeling of

34 Cochleae from hatchling chicks were placed in culture, and hair cells

35 erior rectus and superior oblique muscles of hatchling chicks were treated in vivo either to increase

36 ed in learning of passive avoidance tasks in hatchling chicks.

37 erve and NM on both sides were obtained from hatchling chicks.

38 n the telencephalon are similar in adult and hatchling Columbiformes.

39 Complementarily, in stagnant water, hatchlings covered more ground using hyperstable swimmin

40 alien species, including known predators of hatchling crocodiles (e.g., Clarias sp.) and egg predato

41 sting was chronically blocked with curare in hatchlings, dark-induced expansion of receptive fields w

42 Water quality, and total adult, juvenile and hatchling densities were evaluated.

43 southern Japan is remarkably stable and that hatchling dispersal to oceanic habitats itself does not

44 ovide similarly lipid-rich milk to altricial hatchlings during parental care.

45 was comprised of juveniles, with adults and hatchlings each comprising 25% of the population.

46 e active season (November), an age cohort of hatchlings emerges; larger juveniles or adults are not p

47 to identify fully fledged feathering in the hatchling enantiornithine bird specimen MPCM-LH-26189, s

48 Estrogen treatment of hatchling females caused an increase in the expression o

49 In the spinal cord of hatchling frog tadpoles of unknown sex, we found that th

50 sked how head skin stimuli evoke swimming in hatchling frog tadpoles.

51 These hatchlings grow rapidly, reach sexual maturity in less t

52 Hatchlings had bufadienolides in their nuchal glands onl

53 Hatchlings have smaller antennae with fewer OSNs; removi

54 d survival to be strongly age dependent with hatchlings having the lowest survival rates (16%) but in

55 This increase in effort places these hatchlings in a precarious position; prone to inversion

56 sed to lower metabolic rates and much larger hatchlings in most nautilids may explain the selective e

57 g incubation temperatures on the survival of hatchlings in nests.

58 tance (quadruped/biped) changed in ontogeny, hatchling, juvenile (~1 year old) and adult (8+ years ol

59 close to the origin of Sauropoda known from hatchling, juvenile and mature specimens, providing a su

60 tabolous stick insect (Timema californicum): hatchlings, juveniles, and adults.

61 In hatchlings, Kv1.2 staining decreased in the cell bodies

62 ocations of the amphidial cell bodies in the hatchling larva (L1) were compared with their locations

63 lation of specifically recognized neurons in hatchling larvae (L1) in which neuronal cell bodies are

64 e finger cell neurons (AFD), were ablated in hatchling larvae with a laser microbeam, and these were

65 give rise to a horizontal stripe pattern in hatchling larvae.

66 ple of defensive color switching is found in hatchling lizards, which use conspicuous tail colors to

67 Here we report, however, that hatchling loggerhead sea turtles (Caretta caretta) from

68 Here we report that hatchling loggerheads, when exposed to magnetic fields r

69 HVC and area X by P11, whereas treatment of hatchling males with the aromatase inhibitor fadrozole d

70 Hatchling mass was not affected.

71 ervention to increase the production of male hatchlings may be needed.

72 Hatchling mean in-water swimming speed was 0.25 m/s (+/-

73 termination to a focus on temperature-linked hatchling mortalities.

74 show the generality of relationships between hatchling mortality and incubation temperature and hence

75 Hatchling (n = 42) over-ground and in-water swimming spe

76 uggests that the remains represent precocial hatchlings of enantiornithine birds.

77 ed these hypotheses by testing inexperienced hatchlings of five species of tortoises, solitary animal

78 on to approach face-like stimuli observed in hatchlings of these solitary species suggests the presen

79 officinalis and were compared with those in hatchlings of two other cephalopod species.

80 ees C, temperatures that produce only female hatchlings or a male-biased sex ratio, respectively.

81 ry experiments, if we physically constrained hatchlings or blocked sensations of motion through visio

82 d be revitalised and, as originally planned, hatchlings or juveniles should not be released beyond AN

83 High levels of mortality among nests, hatchlings or maturing turtles produced in the Melbourne

84 he linked effects of warming temperatures on hatchling output and on sex ratios for these species tha

85 Hatchling output increased with long-term precipitation

86 e effect of local climatic conditions on the hatchling output of leatherback turtles (Dermochelys cor

87 High air temperature reduced hatchling output only at the area experiencing seasonal

88 On predator-introduction islands, those hatchling populations were a smaller fraction of pre-hur

89 found that although, ordinarily, cuttlefish hatchlings prefer shrimp-like prey, when visually expose

90 io is currently almost balanced, with 52% of hatchlings produced being female.

91 the climatic variable(s) that best described hatchling production at each nesting beach.

92 cales on loggerhead turtle (Caretta caretta) hatchling production at seventeen nesting beaches in Bah

93 ro, are projected to experience increases in hatchling production by the end of the 21(st) century.

94 kely to provide conditions suitable for male hatchling production in a warming world.

95 It is crucial to understand how the hatchling production of sea turtles is influenced by loc

96 itation were found to be the main drivers of hatchling production throughout Brazil.

97 on hatching success and hatchling viability (hatchling production).

98 hia, are projected to experience declines in hatchling production, while the more temperate nesting b

99 tential changes in climate may impact future hatchling production.

100 oraging females that provide higher rates of hatchling production.

101 son and in shaded areas, will guarantee male hatchling production; (b) IPCC SLR scenarios will lead t

102 also performed feeding experiments in which hatchling R. tigrinus were reared on controlled diets th

103 ields of ganglion cells exposed to curare in hatchlings reared in normal light and dark cycles were s

104 ced hatchling sex ratios of 53% and 63% male hatchlings, respectively, for hawksbill and green turtle

105 motion through vision and the lateral line, hatchlings responded by elevating their buoyancy and pas

106 ipheral and central trigeminal structures in hatchling ring doves.

107 Here, we examine hatchling self-righting performance in three morphologic

108 Here, we reveal hatchling sensorimotor mechanisms for controlling disper

109 For green turtles, when the female bias in hatchling sex ratio was >90%, the incidence of multiple

110 s which would likely produce fairly balanced hatchling sex ratios of 53% and 63% male hatchlings, res

111 eratures at nest depths and implications for hatchling sex ratios of hawksbill turtles (Eretmochelys

112 ates should be selected not only to maintain hatchling sex ratios, but also to minimize nest removal

113 populations with more extreme female-biased hatchling sex-ratio skews.

114 t microtubule-associated protein 2 (MAP2) in hatchlings showed that some Kv1.1 remained as clusters w

115 ng, developmental periods are 20% longer and hatchling sizes are slightly (~1%) smaller on average th

116 hal warming decreased embryonic survival and hatchling sizes.

117 ios, primarily using data from embryonic and hatchling specimens of Pterodaustro guinazui and Sinopte

118 Notably, in hatchlings, spontaneous and odor-evoked firing rates of

119 oduction and fertility resulted in decreased hatchling success (p = 0.023).

120 anagement practices are focused on nests and hatchling survival; however, protection efforts that ext

121 and three (13%) produced germline transgenic hatchlings that expressed the GFP protein (F1).

122 annibalism-a strong attraction to vulnerable hatchlings-that is absent in the native range.

123 Finally, in the hatchling, the vast majority of principal cells is capab

124 both age groups, though they were smaller in hatchlings, they were proportional to overall brain size

125 sequenced transcripts from embryos, one-day hatchlings, three nymphal stages, and male and female ad

126 Precocial avian hatchlings thus likely play a more active role in direct

127 a biological means used by extant sea turtle hatchlings to elevate metabolic and growth rates - had e

128 oss-fostered eggs and tested the response of hatchlings to the scent of genetic vs. foster parents.

129 on, Pipiscius, and Priscomyzon), including a hatchling-to-adult growth series of the genus Priscomyzo

130 e, including effects on hatching success and hatchling viability (hatchling production).

131 The microbiome of the hatchlings was dominated by a specific, but undescribed,

132 In this study, leatherback hatchlings were actively tracked with miniature acoustic

133 The lower in-water speed suggests hatchlings were advected by the currents, with overall m

134 A 'flap-early' model proposes that hatchlings were capable of independent life and flapping

135 We demonstrate that these hatchlings were capable of rapid self-righting and used

136 Hatchlings were exposed to two nitrate concentrations co

137 Over the study period, 7,427 hatchlings were marked and 380 individuals were recaptur

138 natal dinosaurs suggests that known dinosaur hatchlings were precocial.

139 A minimum of 529 hatchlings were produced on Ile aux Aigrettes in 11 year

140 Naive hatchlings will feed and grow successfully on many diffe

141 tered their behavior and resulted in smaller hatchlings with reduced yolk sac volumes.

142 destabilized stepping in posthatching day 8 hatchlings, with occasional collapses, variable step pro

143 By studying simple hatchling Xenopus laevis tadpoles, we have already ident

144 When the hatchling Xenopus tadpole swims, responses to cutaneous

145 erneurons that drive the swimming CPG in the hatchling Xenopus tadpole, may contribute to the mainten

146 swimming is initiated by tail stimulation in hatchling Xenopus tadpoles, the first trunk contraction

147 a subset of turtles (n = 513), we estimated hatchling yields associated with each hotspots.

148 he synthesis of DHT from testosterone (T) in hatchling zebra finches.